Dutch nOcturnal and hoME dialysis Study To Improve Clinical Outcomes
- Conditions
- CKD, Home Dialysis, Peritoneal Dialysis, Home Haemodialysis, PROMs, Quality of Life, Cost-effectiveness, ESRD, RenalReplacement Therapy.<br />nierfalen, chronische nierschade, thuisdialyse, peritoneale dialyse, thuishaemodialyse, kwaliteit van leven, kosteneffectiviteit, nierfunctievervangende therapie.
- Registration Number
- NL-OMON23350
- Lead Sponsor
- VU University Medical Center Amsterdam (VUmc)<br>University Medical Center Utrecht (UMCU)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 1600
Inclusion Criteria
Age > 18 years
- indication to start with RRT
Exclusion Criteria
- unwillingness to provide informed consent
- life expectancy < 3 months
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of life, obtained from the following questionnaires: SF-12, Dialysis Symptom Index and EQ5D-5L<br><br>
- Secondary Outcome Measures
Name Time Method clinical outcomes (phosphate and anaemia control, nutritional status, infectious complications, hospitalisation, mortality) and cost-effectiveness.